ncbi / magicblast
☆36Updated 2 weeks ago
Alternatives and similar repositories for magicblast:
Users that are interested in magicblast are comparing it to the libraries listed below
- Test data for MultiQC.☆22Updated this week
- Miscellaneous Bioinformatics scripts etc mostly in Python☆45Updated 3 weeks ago
- ☆14Updated 6 years ago
- Project Manager for NGS data analysis☆30Updated 2 years ago
- A toolkit for annotation of transposable element families from unassembled sequence reads☆30Updated 2 years ago
- De novo transcriptome assembler for short reads☆62Updated 7 years ago
- Pauvre: QC and genome browser plotting Oxford Nanopore and PacBio long reads.☆54Updated 5 months ago
- Ococo: the first online variant and consensus caller. Call genomic consensus directly from an unsorted SAM/BAM stream.☆47Updated 6 years ago
- utilities for indexing and sequence extraction from FASTA files☆59Updated 3 years ago
- Modules to interface with tools used in Ensembl Gene Annotation Process and scripts to run pipelines☆18Updated this week
- conda recipes for genomic data☆85Updated 3 years ago
- A Teaching Engine for Genomics☆12Updated 4 years ago
- A collection of publications on comparison of high-throughput sequencing technologies.☆27Updated 4 months ago
- REINDEER REad Index for abuNDancE quERy☆57Updated 9 months ago
- Error correction for Illumina RNA-seq reads☆66Updated last year
- small RNA analysis from NGS data☆37Updated 8 months ago
- Histosketching Using Little Kmers☆56Updated last year
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆55Updated 7 years ago
- Malleable All-seeing Journal Of Research Artifacts☆36Updated last year
- Tools for the analysis of structural variation in genomes☆79Updated last year
- An easy to use and comprehensive python package which aids in the analysis and visualization of orthologous genes. 🐵☆28Updated 4 months ago
- Genome inference from a population reference graph☆96Updated last month
- The command-line interface to GGD☆42Updated 2 years ago
- A method for variant graph genotyping based on exact alignment of k-mers☆86Updated 6 years ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated last week
- A web wrapper for GeneValidator☆11Updated 4 years ago
- Kmer-db is a fast and memory-efficient tool for large-scale k-mer analyses (indexing, querying, estimating evolutionary relationships, et…☆89Updated 5 months ago
- PacBio BAM C++ library☆21Updated last year
- A Python library for reading and writing PacBio® data files☆39Updated 2 months ago
- A set of workflows written in Nextflow for Genome Annotation.☆45Updated 10 months ago